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Authors
Chan, Joe Kwun Nam
Lee, Krystal Chi Kei
Correll, Christoph U. https://orcid.org/0000-0002-7254-5646
So, Yuen Kiu
Chan, Ching Yui
Wong, Corine Sau Man https://orcid.org/0000-0003-3363-1004
Cheung, Ka Wang
Seto, Mimi Tin-Yan
Lin, Jessie
Chang, Wing Chung https://orcid.org/0000-0002-3581-8895
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Funding
Funding for this research was provided by:
Research Grants Council, University Grants Committee (17127417)
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Article History
Received: 16 January 2024
Revised: 19 August 2024
Accepted: 23 August 2024
First Online: 2 September 2024
Competing interests
: CUC has been a consultant and/or advisor to or has received honoraria from: AbbVie, Acadia, Adock Ingram, Alkermes, Allergan, Angelini, Aristo, Biogen, Boehringer-Ingelheim, Bristol-Meyers Squibb, Car dio Diagnostics, Cerevel, CNX Therapeutics, Compass Pathways, Darnitsa, Delpor, Denovo, Gedeon Richter, Hikma, Holmusk, IntraCellular Therapies, Jamjoom Pharma, Janssen/J&J, Karuna, LB Pharma, Lundbeck, MedAvante-ProPhase, MedInCell, Merck, Mindpax, Mitsubishi Tanabe Pharma, Mylan, Neurocrine, Neurelis, Newron, Noven, Novo Nordisk, Otsuka, Pharmabrain, PPD Biotech, Recordati, Relmada, Reviva, Rovi, Sage, Seqirus, SK Life Science, Sumitomo Pharma America, Sunovion, Sun Pharma, Supernus, Tabuk, Takeda, Teva, Tolmar, Vertex, and Viatris. He provided expert testimony for Janssen and Otsuka. He served on a Data Safety Monitoring Board for Compass Pathways, Denovo, Lundbeck, Relmada, Reviva, Rovi, Supernus, and Teva. He has received grant support from Janssen and Takeda. He received royalties from UpToDate and is also a stock option holder of Cardio Diagnostics, Kuleon Biosciences, LB Pharma, Mindpax, and Quantic. The other authors declare no competing interests. The authors alone are responsible for the content and writing of the paper.
: The study was approved by the Institutional Review Board of the University of Hong Kong/Hospital Authority Hong Kong West Cluster (UW 18-654). All methods adopted by the study were conducted in accordance with the Declaration of Helsinki. As the study was based on a health-record database, the requirement for informed consent was waived. There were no identifiable images from human research participants published in the study and thus no written informed consent for publication of the images would be required.
